An epoxygenase metabolite of DHA
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(±)10(11)-DiHDPA

Item No. 18174

Technical Information
Formal Name
(±)10,11-dihydroxy-4Z,7Z,13Z,16Z,19Z-docosapentaenoic acid
CAS Number
1345275-22-0
Synonyms
  • (±)10,11-DiHDPE
Molecular Formula
C22H34O4
Formula Weight
Purity
≥98%
A 500 µg/ml solution in ethanol
DMF: 50 mg/mlDMSO: 50 mg/mlEthanol: 50 mg/mlPBS (pH 7.2): 0.25 mg/ml
SMILES
CC/C=C\C/C=C\C/C=C\C[C@@H](O)[C@H](O)C/C=C\C/C=C\CCC(O)=O
InChi Code
InChI=1S/C22H34O4/c1-2-3-4-5-6-7-8-11-14-17-20(23)21(24)18-15-12-9-10-13-16-19-22(25)26/h3-4,6-7,10-15,20-21,23-24H,2,5,8-9,16-19H2,1H3,(H,25,26)/b4-3-,7-6-,13-10-,14-11-,15-12-/t20-,21-/m1/s1
InChi Key
OAZUCYZBXHOCES-QBEJVNRSSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Wet ice in continental US; may vary elsewhere
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    Product Description

    (±)10(11)-DiHDPA is produced from cytochrome P450 epoxygenase action on docosahexaenoic acid (DHA; Item No. 90310). It has been shown to inhibit VEGF-induced angiogenesis in mice and may have additional anti-inflammatory and anti-tumor effects.1,2

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Zhang, G., Panigrahy, D., Mahakian, L.M., et alEpoxy metabolites of docosahexaenoic acid (DHA) inhibit angiogenesis, tumor growth, and metastasis. Proc. Natl. Acad. Sci. USA 110(16), 6530-6535 (2013).

    2. Zhang, G., Kodani, S., and Hammock, B.D. Stabilized epoxygenated fatty acids regulate inflammation, pain, angiogenesis and cancer. Prog. Lipid Res. 53, 108-123 (2014).